神经树醇、环磷酰胺及其联合对乳腺癌细胞系MCF-7的抗癌作用。

IF 3.5 4区 医学 Q2 ONCOLOGY
Md Tousif, Masood Nadeem, Ms Tabassum, M Moshahid Alam Rizvi, Syed Ehtaishamul Haque
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引用次数: 0

摘要

在癌症治疗中,像环磷酰胺(CP)这样的化疗药物是最常用的药物,但它的副作用限制了它的应用。因此,开发高效、无副作用或副作用最小的抗癌药物是当务之急。近年来,天然生物活性物质因其高效、安全、经济等优点而受到越来越多的关注。我们之前证明了橙花醇(NER),一种天然衍生的倍半萜醇是一种天然生物活性化合物,可以显著降低cp诱导的瑞士白化小鼠器官毒性。因此,在本研究中,我们打算在密歇根癌症基金会-7 (MCF-7)乳腺癌细胞系中评估NER单独的抗癌特性及其与CP联合的增强作用。MCF-7是应用最广泛的人类乳腺癌细胞系之一,主要是因为它与雌激素受体阳性(ER+)、发光型乳腺癌非常相似,在临床乳腺癌病例中占很大比例(~ 70%)。MCF-7细胞也是非侵入性和低侵袭性的,这使得它们适合用于早期肿瘤建模和细胞毒性筛选。它为评价抗癌药物的疗效提供了一个具有良好特征和临床相关性的模型。通过MTT试验、克隆生成试验、细胞毒性试验、伤口愈合试验和细胞周期阻滞来确定NER、CP及其联合对MCF-7细胞的抗癌特性。4', 6-二氨基-2-苯基吲哚(DAPI)检测核形态变化,评估细胞凋亡。在IC50浓度下,NER、CP及其组合对MCF-7细胞具有细胞毒性,抑制MCF-7细胞的集落形成和迁移,并分别将细胞周期阻滞在G0/G1期、G2/M期和S期。因此,无论是单独给药还是联合给药,NER、CP和它们的联合治疗都显示出对MCF-7细胞的抗癌特性,但联合治疗被证明是最好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticancer efficacy of nerolidol, cyclophosphamide, and their combination against breast cancer cell line MCF-7.

In cancer, chemotherapeutic agents like cyclophosphamide (CP), is the most frequently used drug but the side effects caused by it, limits it's application. Therefore, creation of anticancer medicines with high efficacy and no or minimum side effects is a priority. In recent times, research on natural bioactive has been increased since they are efficient, safe, and economical. We earlier proved that Nerolidol (NER), a naturally derived sesquiterpene alcohol is a natural bioactive compound that could significantly reduce the CP-induced organ toxicities in Swiss albino mice. Thus, in this study, we intended to evaluate the anti-cancer property of NER alone and its potentiating effect in combination with CP in Michigan Cancer Foundation-7 (MCF-7) breast cancer cell line. MCF-7 is one of the most extensively used human breast cancer cell line, primarily because it closely resembles estrogen receptor-positive (ER+), luminal-type breast cancer, which accounts for a significant proportion (~ 70%) of clinical breast cancer cases. MCF-7 cells are also non-invasive and less aggressive, which makes them suitable for early-stage tumor modelling and cytotoxicity screening. It provides a well-characterized and clinically relevant model for evaluating the efficacy of anticancer agents. MTT assay, clonogenic assay, cytotoxicity, wound healing assay, and cell cycle arrest was assessed to determine the anticancer properties of NER, CP, and their combination against MCF-7 cells. The change in nuclear morphology was determined by 4', 6-diamidino-2- phenylindole (DAPI) to assess apoptosis. The NER, CP, and their combination at IC50 concentration was found to be cytotoxic against MCF-7 cells, inhibited colony formation, migration of MCF-7 cells and arrested the cell cycle at G0/G1, G2/M, and S phase, respectively. Thus, NER, CP, and their combination showed anticancer property against MCF-7 cells, when administered alone or in combination, but the combination treatment proved to be the best.

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来源期刊
Medical Oncology
Medical Oncology 医学-肿瘤学
CiteScore
4.20
自引率
2.90%
发文量
259
审稿时长
1.4 months
期刊介绍: Medical Oncology (MO) communicates the results of clinical and experimental research in oncology and hematology, particularly experimental therapeutics within the fields of immunotherapy and chemotherapy. It also provides state-of-the-art reviews on clinical and experimental therapies. Topics covered include immunobiology, pathogenesis, and treatment of malignant tumors.
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